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Data updated: Jun 28, 2026

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU

Biotech
Oncology Execution: Good

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU is a biotechnology company focused on Oncology.

2024
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

FDA Novel Drug Designations

(2024)
1 Novel 1 First-in-Class 1 Breakthrough 1 Fast Track
See 1 novel approval →
2024 ANKTIVA (nogapendekin alfa inbakicept-pmln) First-in-Class · Breakthrough · Fast Track

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's Key Drugs

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's core commercial portfolio centers on ANKTIVA, spanning Oncology — its most strategically important drugs approved in the last 15 years.

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's Recent FDA Approvals

New NDA/BLA approvals for ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's Therapeutic Areas

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's approved drugs and pipeline span 1 therapeutic area, led by Oncology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 100%
1 drugs Phase 1: 10

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's Top Competitors

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Novartis, and Merck. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU Pipeline Snapshot

ALTOR BIOSCIENCE, LLC, AN INDIRECT WHOLLY-OWNED SU has 10 active clinical programs from ClinicalTrials.gov — 0 Phase 3, 0 Phase 2 and 10 Phase 1.

0
Phase 3
0
Phase 2
10
Phase 1

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • ANKTIVA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 0/0 completed
  • Speed: 45 months avg
Unlock Full Intelligence

Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges